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The Breast Cancer Oncogene Ikkε Coordinates Mitochondrial Function and Serine Metabolism

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The Breast Cancer Oncogene Ikkε Coordinates Mitochondrial Function and Serine Metabolism bioRxiv preprint doi: https://doi.org/10.1101/855361; this version posted November 26, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. The breast cancer oncogene IKKε coordinates mitochondrial function and serine metabolism Ruoyan Xu1♯, William Jones1♯, Ewa Wilcz-Villega1, A. Sofia H. Costa3, Vinothini Rajeeve2, Robert B. Bentham4,5, Kevin Bryson6, Ai Nagano1, Busra Yaman1, Sheila Olendo Barasa1, Yewei Wang1, Claude Chelala1, Pedro Cutillas2, Gyorgy Szabadkai4,5,7, Christian Frezza3 & Katiuscia Bianchi1* 1Centre for Molecular Oncology, Barts Cancer Institute, Queen Mary University of London, John Vane Science Centre, Charterhouse Square, London EC1M 6BQ, UK 2Centre for Haemato-Oncology, Barts Cancer Institute, Queen Mary University of London, John Vane Science Centre, Charterhouse Square, London EC1M 6BQ, UK. 3Medical Research Council Cancer Unit, University of Cambridge, Hutchison/MRC Research Centre, Cambridge, United Kingdom. 4Department of Cell and Developmental Biology, Consortium for Mitochondrial Research, University College London, WC1E 6BT London, UK 5Francis Crick Institute, NW1 1AT, London UK 6Department of Computer Sciences, University College London, London WC1E 6BT, UK 7Department of Biomedical Sciences, University of Padua, 35131 Padua, Italy ♯ These authors contributed equally to the work * Correspondence: [email protected] Running Title: IKKε regulates serine biosynthesis Keywords: IKKε / serine biosynthesis / breast cancer / mitochondrial metabolism / ATF4 1 bioRxiv preprint doi: https://doi.org/10.1101/855361; this version posted November 26, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. ABSTRACT The IκB kinase ε (IKKε) is a key molecule at the crossroads of inflammation and cancer. Known for its role as an activator of NFκB and IRF3 signalling leading to cytokine secretion, the kinase is also a breast cancer oncogene, overexpressed in a variety of tumours. However, to what extent IKKε remodels cellular metabolism is currently unknown. Here we used a combination of metabolomics and phosphoproteomics to show that IKKε orchestrates a complex metabolic reprogramming that affects mitochondrial metabolism and serine biosynthesis. Acting independently of its canonical signalling role, IKKε upregulates the serine biosynthesis pathway (SBP) mainly by limiting glucose and pyruvate derived anaplerosis of the TCA cycle. In turn, this elicits activation of the transcription factor ATF4 and upregulation of the SBP genes. Importantly, pharmacological inhibition of the IKKε-induced metabolic phenotype reduces proliferation of breast cancer cells. Finally, we show that in a set of basal ER negative and highly proliferative human breast cancer tumours, IKKε and PSAT1 expression levels are positively correlated corroborating the link between IKKε and the SBP in the clinical context. 2 bioRxiv preprint doi: https://doi.org/10.1101/855361; this version posted November 26, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. INTRODUCTION Chronic inflammation, triggered by the tumour stroma or driven by oncogenes, plays a central role in tumour pathogenesis (Netea et al, 2017). A key step leading to inflammation in both compartments is activation of the transcription factor Nuclear Factor κB (NFκB), mediated via canonical or alternative, non-canonical pathways. Key players in both pathways are the members of the IκB kinase (IKK) family, which, by phosphorylating IκB, induce its proteasome-mediated degradation, a step required for releasing NFκB from the IκB-imposed cytosolic localization and thus leading to its nuclear translocation (Clément et al, 2008). Evidence in support of the crucial role played by the IKK family in inflammation- induced malignant transformation was provided by the reduction of tumour incidence following the deletion of the canonical IKK family member IKKβ in intestinal epithelial and myeloid cells in a mouse model of colitis associated cancer development (Greten et al, 2004). Soon after, the non-canonical member of the IKK family, IKKε, was shown to induce breast cancer (Boehm et al, 2007) and to be overexpressed in ovarian (Guo et al, 2009), prostate (Péant et al, 2011) and non-small cell lung cancers (Guo et al, 2013), pancreatic ductal carcinoma (Cheng et al, 2011), and glioma (Guan et al, 2011). In particular, IKKε was shown to induce breast cancer via mechanisms involving CYLD (Hutti et al, 2009) and TRAF2 (Zhou et al, 2013), ultimately mediating NFκB activation (Boehm et al, 2007). Beyond cancer, IKKε is a key regulator of innate and adaptive immunity, activating NFκB and Interferon Regulatory factor 3 (IRF3), inducing type I interferon (Clément et al, 2008; Zhang et al, 2016), but activation of the interferon response has been reported not to be essential for IKKε-mediated cellular transformation (Boehm et al, 2007). On the other hand, IKKε has been shown to regulate central carbon metabolism both in immune and cancer cells. In dendritic cells (DCs), IKKε, together with its closest homologue TANK binding kinase 1 3 bioRxiv preprint doi: https://doi.org/10.1101/855361; this version posted November 26, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. (TBK1), is required for the switch to aerobic glycolysis induced by activation of the Toll-like receptors (TLRs) and activation of DC. Glycolysis is the main glucose catabolic pathway, whereby through a series of reactions cells metabolise glucose to pyruvate, which, in the presence of oxygen, is in turn oxidised to CO2 in the mitochondrial matrix via the TCA cycle to produce ATP using the mitochondrial respiratory chain. Lack of oxygen prevents the mitochondrial utilization of pyruvate, and glucose is converted into lactate (anaerobic glycolysis). In contrast, aerobic glycolysis refers to a metabolic condition whereby glucose is not fully oxidised in the mitochondria, even in the presence of oxygen, and is utilised for the production of amino acids, lipids and nucleotides via pathways branching out from the glycolysis and TCA cycle. Accordingly, aerobic glycolysis in DCs allows fatty acids synthesis, which is required for the expansion of the endoplasmic reticulum and Golgi, supporting DC activation (Everts et al, 2014). Allowing the production of key cellular constituents, aerobic glycolysis is most frequently observed in highly proliferative cells, such as activated immune cells and cancer cells (Andrejeva & Rathmell, 2017). Accordingly, IKKε also regulates glucose uptake in pancreatic ductal adenocarcinoma as well as mitochondrial function in mouse embryonic fibroblasts (MEFs) (Zubair et al, 2016; Reilly et al, 2013). However, a comprehensive investigation of the role of IKKε as regulator of cellular metabolism in cancer has not yet been carried out. The serine biosynthesis pathway (SBP) is known to be dysregulated in cancer as target of a series of oncogenes (Amelio et al, 2014; Yang & Vousden, 2016), and phosphoglycerate dehydrogenase (PHGDH), the first enzyme of the pathway, is amplified in breast cancer and melanoma, where it functions as an oncogene (Locasale et al, 2011; Possemato et al, 2011). However, whether inflammatory signalling regulates the SBP pathway to promote tumorigenesis has not yet been investigated. 4 bioRxiv preprint doi: https://doi.org/10.1101/855361; this version posted November 26, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Considering the emerging role of IKKε in inflammation and breast tumorigenesis, where the SBP has a known pro-oncogenic role, we investigated the potential intersection between IKKε−mediated inflammatory pathways and the SBP. We found that IKKε directly controls the SBP via activation of a mitochondria-nuclear retrograde pathway and the transcription factor ATF4, leading to upregulation of the SBP enzymes, in particular phosphoserine aminotransferase 1 (PSAT1). Importantly we also demonstrate that IKKε- mediated regulation of cellular metabolism is independent of the canonical signalling pathway via NFκB/IRF3. Moreover, we have identified a subset of basal, estrogen receptor negative (ER-) highly proliferative breast tumours where IKKε and PSAT1 expression correlates, confirming the pathophysiological role of our findings. These results identify an additional role for IKKε in breast cancer, adding regulation of cellular metabolism to the canonical oncogenic pathways. Thus, our data suggest a synergistic mechanism of action by which alterations of cellular metabolism and inflammation driven by the IKKε oncogene support tumour growth and proliferation. RESULTS IKKε rewires cellular metabolism To investigate the effect
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